在COPD患者中,奥替特罗/噻托溴铵和维兰特罗/乌莫列地铵的比较疗效:一项与美国医疗保险人群中新用户队列研究相匹配的高维倾向评分

IF 2.7 Expert review of respiratory medicine Pub Date : 2024-12-01 Epub Date: 2024-12-30 DOI:10.1080/17476348.2024.2446598
Chintal H Shah, Robert M Reed, Linda Wastila, Eberechukwu Onukwugha, Mathangi Gopalakrishnan, Zafar Zafari
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引用次数: 0

摘要

背景:两种长效毒蕈碱拮抗剂吸入器固定剂量组合(奥替特罗/噻托溴铵(OLO/TIO)和维兰特罗/乌莫克利地铵(VI/UMEC))每天一次用于治疗慢性阻塞性肺疾病(COPD)。本研究旨在比较这些吸入器在美国医疗保险人群中预防严重COPD恶化的临床有效性。研究设计和方法:使用具有全国代表性的医疗保险数据(2013-2019),我们在65岁及以上COPD患者中采用了一个新的用户,主动比较设计。关注的结果是首次发生严重COPD恶化的时间。为了确保组间的可比性,我们基于他们的高维倾向得分进行了1:3 (VI/UMEC:OLO/TIO)最近邻匹配。结果:共纳入2263个OLO/TIO新引发剂与6789个VI/UMEC新引发剂匹配。在新启动者中,首次严重COPD恶化的发生率为40.8 / 100人年(OLO/TIO为39.9 / 100人年,VI/UMEC为41.1 / 100人年)。与VI/UMEC相比,启动OLO/TIO的患者首次COPD加重时间的调整风险比为0.948(95%可信区间:0.813-1.105)。结论:在65岁及以上的Medicare COPD患者中,我们未发现OLO/TIO和VI/UMEC新使用者在首次严重恶化时间方面存在统计学差异。
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Comparative effectiveness of olodaterol/tiotropium and vilanterol/umeclidinium among COPD patients: a high-dimensional propensity score matched new user cohort study in a US medicare population.

Background: Two long-acting muscarinic antagonist inhaler fixed dose combinations (olodaterol/tiotropium (OLO/TIO) and vilanterol/umeclidinium (VI/UMEC)) have once-a-day dosing for managing chronic obstructive pulmonary disease (COPD). This study aimed to compare clinical effectiveness of these inhalers in terms of ability to prevent severe COPD exacerbations in a United States Medicare population.

Research design and methods: Using nationally representative Medicare data (2013-2019), we employed a new user, active comparator design among beneficiaries aged 65 years and older with COPD. The outcome of interest was time to first occurrence of a severe COPD exacerbation. To ensure comparability between the groups, we performed 1:3 (OLO/TIO:VI/UMEC) nearest neighbor matching based on their high-dimensional propensity scores.

Results: The study included 2,263 OLO/TIO new initiators matched to 6,789 VI/UMEC new initiators. The incidence rate of the first severe COPD exacerbation was 40.8 per 100 person-years among new initiators (39.9 per 100 person-years for OLO/TIO, 41.1 per 100 person-years for VI/UMEC). The adjusted hazard ratio of the time to first COPD exacerbation was 0.948 (95% Confidence interval: 0.813-1.105) for individuals initiating OLO/TIO versus VI/UMEC.

Conclusion: We did not find a statistically significant difference between the OLO/TIO and VI/UMEC new users in terms of time to first severe exacerbation among Medicare COPD patients aged 65 or older.

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